Acute Rheumatism

Total Page:16

File Type:pdf, Size:1020Kb

Acute Rheumatism Ann. rheum. Dis. (1970), 29, 569 Ann Rheum Dis: first published as 10.1136/ard.29.5.569 on 1 September 1970. Downloaded from Abstracts This section is published in collaboration with Abstracts of World Medicine and Ophthalmic Literature, published by the British Medical Association, and also includes a great many which are specially commissioned for this Journal. They are divided into the following sections: Acute Rheumatism Other Forms of Arthritis Immunology and Serology Rheumatoid Arthritis Bone Diseases Biochemical Studies Still's Disease Non-articular Rheumatism, including Disk Therapy Osteoarthrosis Syndromes, Sciatica, etc. Surgery Spondylitis Pararheumatic (Collagen) Diseases Other General Subjects Gout Connective Tissue Studies At the end of each section is a list of titles of articles noted but not abstracted. Not all sections may be represented in any one issue. Acute rheumatism published in the past, this is the first from Iran, and it emanates from the Pahlavi University School of Medical A Day Hospital for Children with Rheumatic Fever (Paediatric) Cardiology in Shiraz. The prevalence of SPAGNUOLO, M., GAVRIN, J., and RYAN, J. (1970) rheumatic fever over a 10-year period was found to be Pediatrics, 45, 276 1 fig., 11 refs 0 5 per cent., which is higher than that currently reported by copyright. from most Western In the rheumatic disorders of children, as in other ill- countries. In forty episodes observed nesses, the amount of medical supervision needed de- amongst patients of an average age of 10 years, 45 had creases with time, although continued observation re- established carditis (64-5 per cent.), but very few de- mains desirable. The need to avoid the overuse of specia- veloped chorea. Of 55 patients totalling seventy hospital lized and expensive hospital facilities, has led to the admissions, eight died, a case fatality rate of 14-2 per establishment in several places of Day Hospitals, upon cent. No significant difference in socioeconomic status an experimental basis. This report is from the Irvington was detected between the rheumatic and control groups; House contrary to the widely held impression that the disease Day Hospital, New York, where the patients is more frequent in environments in which malnutrition, have the benefit of whatever medical attention and poverty, and overcrowding are prevalent. auxiliary services may be needed and can return home http://ard.bmj.com/ at night. W. S. C. COPEMAN The authors report on one hundred consecutive chil- Role of Tonsils in predisposing to Streptococcal Infections dren with acute rheumatic fever who attended during the and Recurrences of Rheumatic Fever FEINSTEIN, A. R., latter part of their illness at a time when they were able and LEvIrr, M. (1970) New Engl. J. Med., 282, 285 1 to tolerate near-normal activities. Most of them were fig., bibl. finally discharged shortly after discontinuation oftherapy, (see Abstr. Wld Med. (1970), 44, 454). although a few of the exceptions who are described had to be readmitted with clinical rebounds and other Indirect Immunofluorescence in the Serological Diagnosis on September 28, 2021 by guest. Protected residual disorders. of Streptococcal Diseases L. Application in Rheumatic The incidence of permanent heart disease in those Fever (L'immunofluorescenza indiretta nella diagnosi who attended the day hospital did not differ from that sierologica delle affezioni streptococciche. I. Utilizza- in children who had been subjected to full hospitalization zione nella malattia reumatica) CIAMPOLINI, M., for the entire duration of their illness. The authors con- FRANCHINI, F., and TREVISAN, C. (1969). Minerva clude that a long period of hospital care and convales- pediat., 21, 2431 4 figs, 43 refs cence is required only in that 5 per cent. of patients who (See Abstr. Wld Med., (1970) 44, 503.) have chronic rheumatic fever. The others who attended the Day Hospital were able to resume normal activities Decreasing Incidence of a History of Acute Rheumatic including schooling much sooner than if they had con- Fever inChronicRheumaticHeart Disease VENDSBORG, P., tinued as in-patients. W. S. C. COPEMAN FAUERHOLDT-HANSEN, L., and OLESEN, K. H. (1968) Cardiologia, 53, 332 2 figs, 22 refs Acute Rheumatic Fever in Shiraz, Iran GHARIB, R. (See Abstr. Wld Med. (1970), 44, 548). (1969) Amer. J. Dis. Child., 118, 694 24 refs Some Aspects of Epidemiology and Surveillance of Although reports upon the incidence of rheumatic Rheumatic Fever 9rrAj, S., URBANEK, T., and BO§MAN- fever in several of the Middle Eastern countries have been SKY, K. (1970) Acta rheum. scand., 16, 30 4 figs, 20 refs 570 Annals of the Rheumatic Diseases Ann Rheum Dis: first published as 10.1136/ard.29.5.569 on 1 September 1970. Downloaded from Rheumatic Mitral Valvular Disease in the Adolescent. than in the control group. The authors conclude that Clinical Evaluation and Surgical Indications in 86 Cases most-but not all-heart disease found in rheumatoid (Valvulopatia mitral reumdtica del adolescent) MATA, arthritis patients is innocuous. W. S. C. COPEMAN M. L. A., SALOM6N, C. A., and ORDONqEZ, M. A. (1969) Arch. Inst. Cardiol. MWx., 39, 612 5 figs, 16 refs Rheumatoid Arthritis and the Xylose Tolerance Test Studies on the Serum Level of Neuraminic Acid in the GAMBLE, W. S., ABBRUZZESE, A., GRAY, S. J., and Course of Cardiac Failure in Children with Rheumatic BAYLES, T. B. (1969) Amer. J. Gastroent., 52, 445 2 figs, Fever [In Polish] SOWIN'SKA, J., and WOJTECKA, E. 36 refs (1969) Reumatologia (Warsz.), 7, 341 3 figs, 6 refs Among 35 patients with classical or definite rheumatoid arthritis, in whom there was no clinical evidence of Rheumatic Heart Disease Epidemiology. m. The San arteritis or amyloidosis and in whom renal function was Luis Valley Prevalence Study MORTON, W. E., WARNER, grossly normal, the 5-hour urine zylose was significantly A. L., WEIL, J. V., SHMOCK, C. L., JR., SNYDER, J., and reduced (below 6-2 g.) in eighteen, and in six of these LicHTY, J. A. (1970) Circulation, 41, 773 6 refs the serum zylose was raised. A low urine zylose was virtually restricted to females; it was not related to the Rheumatic Fever-1970 LUCKSTEAD, E. F., and DIEHL, titre of rheumatoid serum factor, nor explicable by the A. M. (1970) J. Kans. med. Soc., 71, 97 10 refs use of phenacetin. The authors consider these results to indicate renal impairment rather than intestinal malab- Criteria of Rheumatic Fever DAVIS (1970) Lancet, 1, sorption and suggest that the former may be commoner 1045 than is generally supposed. J. BALL Acute Rheumatic Fever in Virginia-Has it changed in the Last 20 Years? McCuE, C. M., ROBERTSON, L. W., Association of Rheumatoid Arthritis with Plasma Cell and ELDREDGE, W. J., and NOBLE, A. (1970) Virginia med. Lymphocytic Neoplasms GOLDENBERG, G. J., PARAS- Mth., 97, 273 5 figs, 6 refs KEVAS, F., and IsRAELs, L. G. (1969) Arthr. and Rheum. 12, 569-579 6 figs, 36 refs Acid-Base Equilibrium in the Treatment of Rheumatic (See Abstr. Wld Med. (1970), 44, 627) Fever in Children [In Polish] KORYCHA, A., PRONICKA, by copyright. E., JACOBSON, E., and KUBALSKA, J. (1970) Pediat. pol., 45, 413 3 figs, 19 refs Rheumatoid Arthritis, Dysproteinemic Arthropathy, and Paraproteinemia ZAWADZKI, Z. A., and BENEDEK, T. G. Renal Lesions in Rheumatic Heart Disease FAmmy, (1969) Arthr. and Rheum., 12, 555 2 figs, bibl. S. A. (1969) J. Egypt. med. Ass., 52, 524 11 figs, 9 refs (see Abstr. WId Med. (1970), 44, 628) Transient Complete A-V Block in Two Siblings during Association between Rheumatoid Arthritis and Psoriasis in Acute Rheumatic Carditis in Childhood STOCKER et al. Total Populations [In English] HELLGREN, L. (1969) (1970) Pediatrics, 45, 850 Acta rheum. scand., 15, 316 Bibl. (see Abstr. WId Med. (1970), 44, 455) http://ard.bmj.com/ Rheumatoid arthritis Heart Disease in Patients with Sero-positive Rheumatoid Disturbance of Pulmonary Diffusing Capacity in Rheuma- Arthritis BONFIGLIO, T., and ATWATER, E. C. (1969) toid Arthritis and Systemic Lupus Erythematosus (Diffu- Arch. intern. Med., 124, 714 44 refs sionsstorungen bei primarchronischer Polyarthritis und Lupus erythematodes disseminatus) LODDENKEMPER, R., Pericarditis as an autopsy finding in 30 to 40 per cent. of BACH, G. L., and CARTON, R. W. (1970) Beitr. Klin. cases of chronic rheumatoid arthritis has been reported Erforsch. Tuberk., 141, 230 2 figs, 30 refs in many series since Charcot's paper in 1881 which (see Abstr. Wld Med. (1970), 44, 548) on September 28, 2021 by guest. Protected recorded-such a finding in four out of nine examinations. The present authors report detailed post mortem observations in 47 cases of seropositive rheumatoid Studies on the Sicca Syndrome in Patients with Rh toid arthritis and confirm these findings-in an equal number Arthritis ERICSON, S., and SUNDMARK, E. (1970) Acta of unmatched controls it was uncommon. Such lesions, rheum. scand., 16, 60 1 fig., 50 refs although almost always benign, are often associated (see Abstr. Wld Med. (1970), 44, 772) with electrocardiographic changes during life. They also appear to relate to long duration of the arthritis disease Problems of Caplan's Syndrome (Zur Problematik des and severe musculoskeletal disability. Constrictive peri- Caplan-Syndroms) MoRAwErz, F., and ScHNErz, E. carditis and rheumatoid granulomata, however, are (1970) Wien. med. Wschr., 120, 103 4 figs, 17 refs rarely found. Myocarditis was found most frequently in patients with severe osteoporosis. Coronary arteritis, when discovered, seemed to be only doubtfully relevant R atoid Lung Disease (Acute Articular Rh tis) to the rheumatic condition; functionally important (Pneumopathie rhumatismale (Rhumatisme articulaire valvular disease was rate. Non-specific endocarditis, aigu)) CARVALHAL, S. S., ATRA, E., SAAD, F. A., and although found to be quite common, was not more so Pupo, R. A. (1969) Rev. Rhum., 36, 597 9 figs, 15 refs Abstracts 571 Ann Rheum Dis: first published as 10.1136/ard.29.5.569 on 1 September 1970.
Recommended publications
  • Dermatology Eponyms – Sign –Lexicon (P)
    2XU'HUPDWRORJ\2QOLQH Historical Article Dermatology Eponyms – sign –Lexicon (P)� Part 2 Piotr Brzezin´ ski1,2, Masaru Tanaka3, Husein Husein-ElAhmed4, Marco Castori5, Fatou Barro/Traoré6, Satish Kashiram Punshi7, Anca Chiriac8,9 1Department of Dermatology, 6th Military Support Unit, Ustka, Poland, 2Institute of Biology and Environmental Protection, Department of Cosmetology, Pomeranian Academy, Slupsk, Poland, 3Department of Dermatology, Tokyo Women’s Medical University Medical Center East, Tokyo, Japan, 4Department of Dermatology, San Cecilio University Hospital, Granada, Spain, 5Medical Genetics, Department of Experimental Medicine, Sapienza - University of Rome, San Camillo-Forlanini Hospital, Rome, Italy, 6Department of Dermatology-Venerology, Yalgado Ouédraogo Teaching Hospital Center (CHU-YO), Ouagadougou, Burkina Faso, 7Consultant in Skin Dieseases, VD, Leprosy & Leucoderma, Rajkamal Chowk, Amravati – 444 601, India, 8Department of Dermatology, Nicolina Medical Center, Iasi, Romania, 9Department of Dermato-Physiology, Apollonia University Iasi, Strada Muzicii nr 2, Iasi-700399, Romania Corresponding author: Piotr Brzezin′ski, MD PhD, E-mail: [email protected] ABSTRACT Eponyms are used almost daily in the clinical practice of dermatology. And yet, information about the person behind the eponyms is difficult to find. Indeed, who is? What is this person’s nationality? Is this person alive or dead? How can one find the paper in which this person first described the disease? Eponyms are used to describe not only disease, but also clinical signs, surgical procedures, staining techniques, pharmacological formulations, and even pieces of equipment. In this article we present the symptoms starting with (P) and other. The symptoms and their synonyms, and those who have described this symptom or phenomenon. Key words: Eponyms; Skin diseases; Sign; Phenomenon Port-Light Nose sign or tylosis palmoplantaris is widely related with the onset of squamous cell carcinoma of the esophagus.
    [Show full text]
  • Ceratodermia Mutilante De Vohwinkel: Relato De Três Casos Em Uma Família* Vohwinkel´S Mutilating Keratoderma: Report of Three Familial Cases*
    Cavalcante, Holanda, Almeida & Filho 311 Caso Clínico / Case Report Ceratodermia mutilante de Vohwinkel: relato de três casos em uma família* Vohwinkel´s mutilating keratoderma: report of three familial cases* Lúcia Isabel de Sá Cavalcante1 Érica de Magalhães Holanda1 Thereza Lúcia Prata de Almeida 2 José Wilson Accioly-Filho3 Resumo: A ceratodermia hereditária mutilante ou síndrome de Vohwinkel é afecção dermatológica rara caracterizada pelo espessamento cutâneo das palmas, plantas e dorso de mãos e pés, e por constrições em faixa dos dedos (pseudoainhum). São relatados três casos em uma família, envolvendo duas gerações. Em todos havia, adicionalmente, perda auditiva neurossensorial. Discutem-se o diagnóstico diferencial com ou- tras ceratodermias palmoplantares e o tratamento com retinóides. Trata-se da primeira descrição dessa enti- dade no Brasil. Palavras-chave: ainhum; ceratodermia palmar e plantar Summary: Keratoderma hereditarium mutilans, or Vohwinkel´s syndrome, is a rare cutaneous di- sease characterized by thickening of the palms, soles and dorsa of the hands and feet, and by ainhum- like constriction of the fingers. This paper reports a case of three family members, over a span of two generations, who were affected by this disorder. Sensorineural deafness was also observed in each patient. We discuss differential diagnosis and retinoid treatment of this condition. This is the first case report on this disease to come from Brazil. Key words: ainhum; keratoderma, palmoplantar. INTRODUÇÃO INTRODUCTION As ceratodermias palmoplantares hereditárias repre- Heriditary palmoplantar keratodermas represent a sentam um grupo heterogêneo de doenças que se caracteri- heterogeneous group of diseases characterized by diffuse zam pelo espessamento cutâneo difuso ou focal das palmas e or focused cutaneous thickening of the palms and soles.
    [Show full text]
  • Secondary Pseudoainhum in a Patient with Turner Syndrome Brady S
    CASE REPORT Secondary Pseudoainhum in a Patient With Turner Syndrome Brady S. Davis, OMS IV Scott Harris, DO Mitchell D. Forman, DO Report of Case From the Touro University Secondary pseudoainhum is an autoam- A 44-year-old white woman with Turner syndrome Nevada College of putation that develops in individuals aged (45,X) presented for a routine rheumatologic examina- Osteopathic Medicine in Henderson. approximately 20 to 50 years and is caused tion for episodic oligoarthritis in her right ankle. A complete medical history and physical examination re- Financial Disclosures: by diseases such as keratodermas, trauma, or None reported. congenital factors. The authors report a novel vealed bilateral lower extremity toe lesions. Her left second and third, and her right second, third, and fourth Support: None reported. case of secondary pseudoainhum in a patient toes demonstrated linear bandlike constrictions be- Address correspondence with Turner syndrome (45,X) who presented tween the interphalangeal joints (Figure) consistent to Brady S. Davis, OMS IV, with bandlike constrictions in the toes bilat- 874 American Pacific Dr, with grade I pseudoainhum. The toes were warm, non- erally. To the authors’ knowledge, secondary Henderson, NV 89014-8800 tender, and had good capillary refill. There was no pseudoainhum has not been reported to be E-mail: do14.brady.davis clinical evidence to suggest peripheral vascular disease. associated with Turner syndrome. However, @nv.touro.edu The patient could not recall how long the painless, physicians should be aware of this potential- Submitted asymptomatic lesions had been present. She reported October 18, 2013; ly deforming disease in patients with Turner no trauma to the toes or feet.
    [Show full text]
  • Global Development Assistance for Adolescent Health from 2003 to 2015
    Supplementary Online Content Li Z, Li M, Patton GC, Lu C. Global development assistance for adolescent health from 2003 to 2015. JAMA Netw Open. 2018;1(4):e181072. doi:10.1001/jamanetworkopen.2018.1072 eTable 1. List of Donor Countries Included in the CRS eTable 2. 132 Recipients in the CRS (According to the World Health Organization Regions) eTable 3. Key Words to Identify the Related Age Group (Adolescence) in the Creditor Reporting System eTable 4. CRS Purpose Name and Respective Fractions Allocated to Adolescent Health eTable 5. Definitions of DAAH on the Leading Causes of DALYs of Adolescent Health eTable 6. Key Words Used to Search for Projects on Skin and Subcutaneous Diseases in the Creditor Reporting System eTable 7. Key Words Used to Search for Road Injury Projects in the Creditor Reporting System eTable 8. Key Words Used to Search for HIV/AIDS Projects in the Creditor Reporting System eTable 9. Key Words Used to Search for Projects on Iron-Deficiency Anemia in the Creditor Reporting System eTable 10. Key Words Used to Search for Self-Harm Projects in the Creditor Reporting System eTable 11. Key Words Used to Search for Projects on Interpersonal Violence in the Creditor Reporting System eTable 12. Key Words Used to Search for Projects on Depressive Disorders in the Creditor Reporting System eTable 13. Key Words Used to Search for Projects on Lower Back and Neck Pain in the Creditor Reporting System eTable 14. Key Words Used to Search for Diarrheal Projects in the Creditor Reporting System eTable 15. Key Words Used to Search for Tuberculosis Projects in the Creditor Reporting System eTable 16.
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 7,359,748 B1 Drugge (45) Date of Patent: Apr
    USOO7359748B1 (12) United States Patent (10) Patent No.: US 7,359,748 B1 Drugge (45) Date of Patent: Apr. 15, 2008 (54) APPARATUS FOR TOTAL IMMERSION 6,339,216 B1* 1/2002 Wake ..................... 250,214. A PHOTOGRAPHY 6,397,091 B2 * 5/2002 Diab et al. .................. 600,323 6,556,858 B1 * 4/2003 Zeman ............. ... 600,473 (76) Inventor: Rhett Drugge, 50 Glenbrook Rd., Suite 6,597,941 B2. T/2003 Fontenot et al. ............ 600/473 1C, Stamford, NH (US) 06902-2914 7,092,014 B1 8/2006 Li et al. .................. 348.218.1 (*) Notice: Subject to any disclaimer, the term of this k cited. by examiner patent is extended or adjusted under 35 Primary Examiner Daniel Robinson U.S.C. 154(b) by 802 days. (74) Attorney, Agent, or Firm—McCarter & English, LLP (21) Appl. No.: 09/625,712 (57) ABSTRACT (22) Filed: Jul. 26, 2000 Total Immersion Photography (TIP) is disclosed, preferably for the use of screening for various medical and cosmetic (51) Int. Cl. conditions. TIP, in a preferred embodiment, comprises an A6 IB 6/00 (2006.01) enclosed structure that may be sized in accordance with an (52) U.S. Cl. ....................................... 600/476; 600/477 entire person, or individual body parts. Disposed therein are (58) Field of Classification Search ................ 600/476, a plurality of imaging means which may gather a variety of 600/162,407, 477, 478,479, 480; A61 B 6/00 information, e.g., chemical, light, temperature, etc. In a See application file for complete search history. preferred embodiment, a computer and plurality of USB (56) References Cited hubs are used to remotely operate and control digital cam eras.
    [Show full text]
  • Primary Surgery
    811 Make sure the pain is due to the varicose veins (relieved on lying down, worse at the end of a day’s standing), and 35 Vascular surgery not due to (invisible) ischaemia, arthritis of the hip or knee, a prolapsed intervertebral disc, or meralgia paraesthetica (32.17) which can be there at the same time as the (visible) varicose veins. Swelling of the legs may 35.1 Varicose veins co-exist with varicose veins, but is usually due to another cause, e.g. heart failure or lymphoedema. Very occasionally varicose veins are the result of an ANATOMY AND PHYSIOLOGY. arterio-venous fistula: you should be able to hear a bruit There are four categories of leg vein, and they all have valves which stop and feel a thrill over the fistula. The veins may be blood flowing downwards away from the heart. (1) Long and short saphenous veins run superior to the deep fascia, enormous. Occlusion of the fistula by pressure will, and are usually deep to the fibrous layer of the superficial fascia (35-1). however, make them disappear. They have numerous valves, the most important of which is the femoral valve, in the long saphenous vein, just before it penetrates the deep fascia to join the femoral vein. The femoral valve prevents blood from the femoral vein flowing back into the saphenous vein. (2) Superficial collecting veins are tributaries of the saphenous veins. They lie between the skin and the fibrous layer of the superficial fascia. These have valves, but they are poorly supported by connective tissue.
    [Show full text]
  • R Oad M Ap to IC D -10 -C M
    road map Walk Through Skin and Subcutaneous Tissue Crossovers By Deborah Grider, CPC, CPC-H, CPC-P, CEMC, CPC-I, CCS, CCS-P Our journey using the ICD-10-CM roadmap leads The codes in categories L89 Decubitus ulcer and L97 us to draft guidelines and coding issues focusing on Non-decubitus chronic ulcer of lower limb, not elsewhere clas- “Understanding the ICD-10-CM Draft Guidelines for sified contain a great deal of detail. the Skin and Subcutaneous Tissue.” Consider the codes . The fourth character delineates the anatomy for the Skin and Subcutaneous Tissue located in chap- details (right versus left, upper versus lower). ter 12 of ICD-10-CM. The fifth character identifies the ulcer’s specific site. In ICD-9-CM there are three subchapters in chapter 12: . The sixth character identifies ulcer depth. 680–686 Infections of skin and subcutaneous tissue For example: A physician is called by the nursing home 690–698 Other inflammatory conditions of skin and subcutaneous tissue to treat a patient with bed sores on the left buttock. 700–709 Other diseases of skin and subcutaneous tissue After examining the patient, the physician documents decubitus ulcer, left buttock, stage II. These three subchapters were expanded in ICD-10-CM Compare a pressure ulcer (decubitus ulcer) of the chapter 12 to include blocks L00-L99, as follows: left buttock: L00–L08 Infections of the skin and subcutaneous tissue L10–L14 Bullous disorders ICD-9-CM ICD-10-CM L20–L30 Dermatitis and eczema L40–L45 Papulosquamous disorders 707.0 Chronic ulcer of skin L89 Pressure Ulcer
    [Show full text]
  • Evaluation of Acitretin in the Treatment of Multiple Recalcitrant Common Warts: a Pilot Study Eleni Tzouveka* Sygros Hospital, Athens, Greece
    igmentar f P y D l o i a so n r Tzouveka, Pigmentary Disorders 2015, 2:5 r d u e r o J s Journal of Pigmentary Disorders DOI: 10.4172/2376-0427.1000185 ISSN: 2376-0427 Case Report Open Access Evaluation of Acitretin in The Treatment of Multiple Recalcitrant Common Warts: a Pilot Study Eleni Tzouveka* Sygros Hospital, Athens, Greece Abstract Morphea, also known as Localized scleroderma, is an idiopathic often self-limited, inflammatory disorder that causes fibrotic changes in the skin. Fibrotic, asymmetric plaques, usually 2-15 cm wide, characterize the disease. The active lesions may have erythematous or violaceous borders, whereas the inactive ones may result to hyperpigmentation. The thickening may expand to the subcutaneous tissue or may be to the lower layers of the skin, causing dysfunction at certain levels. There is no relevance to any systematic disease. Morphea usually evolves for several years and then degrades. Introduction pathogenesis. This results in the creation of adhesion molecules and T-helper 2 cytokines, such as interleukins IL-4 and IL-6, and Morphea or Localized Scleroderma is a disorder characterized by transforming growth factor-beta [TGF-β]. These cytokines result in excessive deposition of collagen, resulting in thickening of the skin, mobilization of eosinophils, the CD4 + T-cells and macrophages, which the subcutaneous tissue, or both [1-4]. Morphea can be categorized to are present in early lesions of the disease and the Eosinophilic fasciitis certain types: [21,22]. Cytokines along with growth factors increase fibroblastic • Plaque-type morphed, activity and induce further collagen synthesis and connective tissue [23].
    [Show full text]
  • A CASE of CONGENITAL PSEUDO AINHUM by AGNESE M
    A CASE OF CONGENITAL PSEUDO AINHUM By AGNESE M. T. KELLY, M.D., D.C.H. Dermatology Department, Belfast City Hospital THE CHILD referred to in this report was first seen by a surgeon at the age of eleven weeks because of the presence of constricting bands around the base of the right thumb and middle finger, associated with shortening of the left index finger. These features had been present since birth. The surgeon recognised the condition as a form of ainhum and kept the child under review. It was eventually referred to a dermatologist as a matter of interest and was then thought worthy of report because of its comparative rarity. A detailed family history was obtained and a review of the literature undertaken. The recognised varieties of ainhum appear to be as follows: (a) True ainhum. (b) Condition simulating ainhum but due to trauma. (c) Ainhum-like syndrome. (d) Pseudo ainhum. True Ainhum This was first described by Clarke in 1860 among natives of the African Gold Coast and it was designated by him as "a dry gangrene of the little toe". In 1867 da Silva Lima together with Wucherer introduced the term "ainhum". It is a disease of unknown aetiology and is seen almost entirely in dark skinned persons. Usually the fifth toes are involved by a painless progressively constricting band. The degree of the constriction varies greatly. It may be slight or it may progress deeply until there is either spontaneous amputation of the little toe, or the toe may have to be removed surgically because of gangrene.
    [Show full text]
  • Dactylolysis Spontanea): a Rare Cause of Consult in Dermatology- a Case Report and Review of Literature
    Open Access Austin Journal of Dermatology Case Report Ainhum (Dactylolysis Spontanea): A Rare Cause of Consult in Dermatology- A Case Report and Review of Literature González LF1*, González CA2, Motta A1,3 and Rodríguez F4 Abstract 1Dermatology Program, El Bosque University, Colombia Ainhum or Dactylolysis Spontanea is an idiopathic condition due to 2Dermatology Service, Kennedy Hospital, Colombia constriction rings or grooves on the digits that result in auto amputation. The 3Dermatology Service, Simón Bolívar Hospital, Colombia ainhum commonly affects the fifth toe and usually the compromise is bilateral. 4Radiology Service, Colombia Clinic, Colombia This disease affects mainly African American adults between 20 to 50 years old *Corresponding author: Luis Fernando González, from tropical and sub-tropical regions. We report a 75 years-old man with clinical Dermatology Program, El Bosque University, Av. Cra. 9 # and radiographic findings of unilateral ainhum of left fifth toe. 131A 02. Bogotá, Colombia Keywords: Ainhum; Amputation; Dactylolysis spontanea Received: December 19, 2016; Accepted: January 16, 2017; Published: January 19, 2017 Introduction caused by a circular fibrotic constrictive band affecting the digits that result in progressive ischemia and auto amputation [3]. Ainhum The term ainhum or Dactylolysis Spontanea was used for first time may affect any hand fingers [4] or toes [5], commonly the affected by da Silva Lima in 1867 [1,2]. It is believed that the word “ainhum” digit is the fifth toe and usually this compromise is bilateral [3]. The derives from the Brazilian word “Nago” meaning ‘fissure’ or the affected population is African descendent individuals between 20 to Nigerian word “Yoruba” meaning ‘to saw’ [1].
    [Show full text]
  • Perforating Dermatoses
    مـصـر Egypt 3 Dr. Shoukry A. Sakr •Consultant of Dermatology & Cosmetology. •Consultant of Andrology & Marital Relations. •Cairo university , Cairo , Egypt مـصـر Egypt 5 6 OBAGI MEDICAL CENTER KUWAIT 2006-2009 9 Dr. SHOUKRY SAKR ENCYCLOPEDIA WWW.SHOUKRYSAKRDERMAPEDIA.COM SKIN STRUCTURE SKIN STRUCTURE SKIN STRUCTURE Epidermis Vein Dermis Artery Sweat gland Hair follicle Nerve receptor Sebaceous gland 12 Hypodermis EPIDERMAL CELLS 13 EPIDERMAL CELLS 14 EPIDERMAL CELLS 15 THE DERMIS THE DERMIS THE DERMIS THE DERMIS Shaft Sebaceous gland Papilla Sheath Follicle THE DERMIS FUNCTIONS OF THE SKIN 1. The skin is the largest body organ about 6 square meters 2. Body temperature regulation i.e. thermoregulatory function 3. Prevents loss of important body fluids e.g. plasma. 4. Preventing toxic materials to enter into within the tissues. 5. Protects the body from harmful influences of factors like UVR and radiations by (melanocytes) that produce melanin which gives skin , nail and hair color. 6. Works as excretory organ : toxic substances expelled through sweat. 7. Supports and maintains the internal organs of the body. 8. Immune & infection control function. 9. Sensory organ for the pain, heat , cold , touch & pressure. 10. Manufacturer of vitamin "D" under the influence of UVR . 11. Skin is a mirror which reflects expressions as fear or joy . The internal diseases may appear to have cutaneous manifestations. 12. Skin22 texture , color and smell has a very important role in the sexual relations. PERFORATING DERMATOSES 23 PERFORATING DERMATOSES By
    [Show full text]
  • Boards' Fodder
    boards’ fodder Inherited Palmar Plantar Keratodermas Noushin Heidary, BA & Sharon E. Jacob, MD. (Updated July 2015*) GENE(S) MODE OF NAME OF PPK SYNDROME INVOLVED TRANSMISSION CLINICAL MANIFESTATION Acrokeratoelastoidosis Unknown Autosomal Yellow, hyperkeratotic papules (appearing umbilicated) Dominant (AD) on border of palms/soles Bart-Pumphrey syndrome Connexin 26 (GJB2) AD Leukonychia, congenital hearing loss (cochlear) Striate PPK (Brunauer-Fuhs-Siemens Desmoglein 1 AD Linear hyperkeratotic streaks on volar surface of finger syndrome) and palms; no systemic associations Clouston syndrome (hidrotic Connexin 30 (GJB6) AD Diffuse transgrediens PPK, alopecia, nail dystrophy, ectodermal dysplasia) and other anomalies (cataracts, strabismus, tufted terminal phalanges) Darier’s disease ATP2A2 AD Hyperkeratotic papules in seborrheic regions; white and red longitudinal bands, pterigium and V-shaped distal nicking on nails Epidermolysis bullosa simplex Keratin 5/14 AD PPK with traumatic palmoplantar & mucocutaneous associated with PPK blistering Epidermolytic PPK (EPPK) with Keratin 1 AD Chronic diffuse PPK with flares of psoriasiform plaques polycyclic psoriasiform plaques Erythrokeratoderma variabilis Connexins 31 and AD Transient areas of figurate erythema, hyperhidrosis, 30.3 (GJB3 and PPK with transgrediens, hyperkeratotic plaques GJB4) Focal acral hyperkeratosis Unknown AD Crateriform papules showing no elastorrhexis Focal EPPK Unknown AD Focal and painful keratotic lesions, mainly on plantar pressure points Focal NEPPK (non-epidermolytic
    [Show full text]